Originally published as JCO Early Release 10.1200/JCO.2005.06.027 on January 4 2005
Journal of Clinical Oncology, Vol 23, No 9 (March 20), 2005: pp. 1969-1978
© 2005 American Society of Clinical Oncology.
Prognostic Index for Adult Patients With Acute Myeloid Leukemia in First Relapse
Dimitri A. Breems,
Wim L.J. Van Putten,
Peter C. Huijgens,
Gert J. Ossenkoppele,
Gregor E.G. Verhoef,
Leo F. Verdonck,
Edo Vellenga,
Georgine E. De Greef,
Emanuel Jacky,
Johannes Van der Lelie,
Marc A. Boogaerts,
Bob Löwenberg
From the Dutch-Belgian Hemato-Oncology Cooperative Group (HOVON); Swiss Group for Clinical Cancer Research Collaborative Group (SAKK); Department of Hematology and HOVON Data Center, Rotterdam; Department of Hematology, Free University Medical Center Department of Hematology, Academic Medical Center, Amsterdam; Department of Hematology, University Medical Center, Utrecht; Department of Hematology, University Hospital, Groningen, the Netherlands; Department of Hematology, Hospital Gasthuisberg, Leuven, Belgium; and Department of Internal Medicine, University Hospital, Zürich, Switzerland
Address reprint requests to B. Löwenberg, MD, PhD, Erasmus University Medical Center, Department of Hematology, PO Box 2040, 3000 CA Rotterdam, the Netherlands; e-mail: b.lowenberg{at}erasmusmc.nl
PURPOSE: The treatment of acute myeloid leukemia (AML) in first relapse is associated with unsatisfactory rates of complete responses that usually are short lived. Therefore, a clinically useful prognostic index can facilitate therapeutic decision making and evaluation of investigational treatment strategies at relapse of AML.
PATIENTS AND METHODS: A prognostic score is presented based on the multivariate analysis of 667 AML patients in first relapse among 1,540 newly diagnosed non-M3 AML patients (age 15 to 60 years) entered onto three successive Dutch-Belgian Hemato-Oncology Cooperative Group and the Swiss Group for Clinical Cancer Research Collaborative Group trials.
RESULTS: Four clinically relevant parameters are included in this index (ie, length of relapse-free interval after first complete remission, cytogenetics at diagnosis, age at relapse, and whether previous stem-cell transplantation was performed). Using this stratification system, three risk groups were defined: a favorable prognostic group A (overall survival [OS] of 70% at 1 year and 46% at 5 years), an intermediate-risk group B (OS of 49% at 1 year and 18% at 5 years), and a poor-risk group C (OS of 16% at 1 year and 4% at 5 years).
CONCLUSION: The prognostic index estimates the outcome of AML patients in first relapse using four commonly applied clinical parameters and might identify patients who are candidates for salvage and investigational therapy.
Authors' disclosures of potential conflicts of interest are found at the end of this article.

CiteULike Complore Connotea Del.icio.us Digg Facebook Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
J. E. Karp, B. D. Smith, I. Gojo, J. E. Lancet, J. Greer, M. Klein, L. Morris, M. J. Levis, S. D. Gore, J. J. Wright, et al.
Phase II Trial of Tipifarnib as Maintenance Therapy in First Complete Remission in Adults with Acute Myelogenous Leukemia and Poor-Risk Features
Clin. Cancer Res.,
May 15, 2008;
14(10):
3077 - 3082.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Sposto, W. B. London, and T. A. Alonzo
Criteria for Optimizing Prognostic Risk Groups in Pediatric Cancer: Analysis of Data From the Children's Oncology Group
J. Clin. Oncol.,
May 20, 2007;
25(15):
2070 - 2077.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Estey
Acute Myeloid Leukemia and Myelodysplastic Syndromes in Older Patients
J. Clin. Oncol.,
May 10, 2007;
25(14):
1908 - 1915.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. J. Cornelissen, W. L. J. van Putten, L. F. Verdonck, M. Theobald, E. Jacky, S. M. G. Daenen, M. van Marwijk Kooy, P. Wijermans, H. Schouten, P. C. Huijgens, et al.
Results of a HOVON/SAKK donor versus no-donor analysis of myeloablative HLA-identical sibling stem cell transplantation in first remission acute myeloid leukemia in young and middle-aged adults: benefits for whom?
Blood,
May 1, 2007;
109(9):
3658 - 3666.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Jeha and F. J. Giles
Acute myeloid leukemia
ASH Self-Assessment Program,
January 1, 2007;
2007(1):
243 - 252.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Brune, S. Castaigne, J. Catalano, K. Gehlsen, A. D. Ho, W.-K. Hofmann, D. E. Hogge, B. Nilsson, R. Or, A. I. Romero, et al.
Improved leukemia-free survival after postconsolidation immunotherapy with histamine dihydrochloride and interleukin-2 in acute myeloid leukemia: results of a randomized phase 3 trial
Blood,
July 1, 2006;
108(1):
88 - 96.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. W. Milligan, K. Wheatley, T. Littlewood, J. I. O. Craig, A. K. Burnett, and for the NCRI Haematological Oncology Clinical Stud
Fludarabine and cytosine are less effective than standard ADE chemotherapy in high-risk acute myeloid leukemia, and addition of G-CSF and ATRA are not beneficial: results of the MRC AML-HR randomized trial
Blood,
June 15, 2006;
107(12):
4614 - 4622.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. J. Cornelissen and B. Lowenberg
Role of Allogeneic Stem Cell Transplantation in Current Treatment of Acute Myeloid Leukemia
Hematology,
January 1, 2005;
2005(1):
151 - 155.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|